Abstract
Aurantosides G-I (1-3) have been isolated from the lithistid sponge Theonella swinhoei from Papua New Guinea. Their structures were established by spectroscopic and chemical methods. Compounds 1-3 represent new monochloropentaenoyl tetramic acids with mono-, di-, and tri-N-saccharide substituents, respectively. Aurantosides G-I (1-3) failed to show any significant cytotoxicity against the human colon tumor cell line HCT-116.
Publication types
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Animals
-
Antineoplastic Agents / chemistry
-
Antineoplastic Agents / isolation & purification*
-
Antineoplastic Agents / pharmacology
-
Drug Screening Assays, Antitumor
-
Glycosides / chemistry
-
Glycosides / isolation & purification*
-
Glycosides / pharmacology
-
Humans
-
Molecular Structure
-
Nuclear Magnetic Resonance, Biomolecular
-
Papua New Guinea
-
Porifera / chemistry*
-
Pyrrolidinones / chemistry
-
Pyrrolidinones / isolation & purification*
-
Pyrrolidinones / pharmacology
-
Tumor Cells, Cultured
Substances
-
Antineoplastic Agents
-
Glycosides
-
Pyrrolidinones
-
aurantoside G
-
aurantoside H
-
aurantoside I